• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

大分子衰退是人类寿命的终极限制因素。

Macromolecular deterioration as the ultimate constraint on human lifespan.

机构信息

University of Sydney, Australia.

出版信息

Ageing Res Rev. 2011 Sep;10(4):397-403. doi: 10.1016/j.arr.2010.12.001. Epub 2011 Jan 25.

DOI:10.1016/j.arr.2010.12.001
PMID:21272671
Abstract

A number of tissues and organs in the human body contain abundant proteins that are long-lived. This includes the heart, lung, brain, bone and connective tissues. It is proposed that the accumulation of modifications to such long-lived proteins over a period of decades alters the properties of the organs and tissues in which they reside. Such insidious processes may affect human health, fitness and ultimately may limit our lifespan. The human lens, which contains proteins that do not turnover, is used to illustrate the impact of these gradual deleterious modifications. On the basis of data derived from the lens, it is postulated that the intrinsic instability of certain amino acid residues, which leads to truncation, racemisation and deamidation, is primarily responsible for the age-related deterioration of such proteins. Since these post-translational modifications accumulate over a period of many years, they can only be studied using organisms that have lifespans measured in decades. One conclusion is that there may be important aspects of human aging that can be studied only using long-lived animals.

摘要

人体内的许多组织和器官都含有丰富的长寿蛋白质。这包括心脏、肺、大脑、骨骼和结缔组织。据推测,这些长寿蛋白质在几十年的时间里积累的修饰物的积累,改变了它们所在的器官和组织的特性。这种阴险的过程可能会影响人类的健康、健身,最终可能会限制我们的寿命。人类晶状体中含有不会发生转化的蛋白质,它被用来说明这些逐渐产生的有害修饰的影响。基于从晶状体中获得的数据,人们推测,某些氨基酸残基的固有不稳定性,导致截短、消旋和脱酰胺作用,是导致这些蛋白质与年龄相关的恶化的主要原因。由于这些翻译后修饰物在多年的时间里积累,因此只能使用寿命以十年为单位来衡量的生物体进行研究。一个结论是,只有使用长寿动物,才能研究人类衰老的某些重要方面。

相似文献

1
Macromolecular deterioration as the ultimate constraint on human lifespan.大分子衰退是人类寿命的终极限制因素。
Ageing Res Rev. 2011 Sep;10(4):397-403. doi: 10.1016/j.arr.2010.12.001. Epub 2011 Jan 25.
2
Are ancient proteins responsible for the age-related decline in health and fitness?远古蛋白质是否是导致与年龄相关的健康和体能下降的原因?
Rejuvenation Res. 2010 Feb;13(1):83-9. doi: 10.1089/rej.2009.0938.
3
Deamidation of specific glutamine residues from alpha-A crystallin during aging of the human lens.人晶状体老化过程中α-A晶状体蛋白特定谷氨酰胺残基的脱酰胺作用。
Biochemistry. 1998 Sep 29;37(39):13681-5. doi: 10.1021/bi981542k.
4
Cleavage of amino acid residue(s) from the N-terminal region of alpha A- and alpha B-crystallins in human crystalline lens during aging.在衰老过程中,人晶状体中αA-和αB-晶状体蛋白N端区域氨基酸残基的裂解。
Biochem Biophys Res Commun. 1997 Feb 13;231(2):373-8. doi: 10.1006/bbrc.1997.6105.
5
Presbyopia and cataract: a question of heat and time.老花眼和白内障:一个关于热和时间的问题。
Prog Retin Eye Res. 2010 Nov;29(6):487-99. doi: 10.1016/j.preteyeres.2010.05.002. Epub 2010 May 21.
6
Simultaneous stereoinversion and isomerization at the Asp-4 residue in βB2-crystallin from the aged human eye lenses.βB2-晶体蛋白中 Asp-4 残基的同时立体反转和异构化。来自老年人类晶状体。
Biochemistry. 2011 Oct 11;50(40):8628-35. doi: 10.1021/bi200983g. Epub 2011 Sep 14.
7
Molecular signatures of long-lived proteins: autolytic cleavage adjacent to serine residues.长寿蛋白的分子特征:丝氨酸残基附近的自裂解。
Aging Cell. 2012 Dec;11(6):1125-7. doi: 10.1111/j.1474-9726.2012.00860.x. Epub 2012 Aug 23.
8
Increase in the intramolecular disulfide bonding of alpha-A crystallin during aging of the human lens.人晶状体老化过程中α-A晶状体蛋白分子内二硫键的增加。
Exp Eye Res. 1996 Nov;63(5):585-90. doi: 10.1006/exer.1996.0149.
9
Age-related changes in human lens crystallins identified by HPLC and mass spectrometry.通过高效液相色谱法和质谱法鉴定的人晶状体晶状体蛋白的年龄相关变化。
Exp Eye Res. 1998 Jul;67(1):21-30. doi: 10.1006/exer.1998.0482.
10
Ageing and vision: structure, stability and function of lens crystallins.衰老与视力:晶状体晶状体蛋白的结构、稳定性及功能
Prog Biophys Mol Biol. 2004 Nov;86(3):407-85. doi: 10.1016/j.pbiomolbio.2003.11.012.

引用本文的文献

1
Advances in the Study of Protein Deamidation: Unveiling Its Influence on Aging, Disease Progression, Forensics and Therapeutic Efficacy.蛋白质脱酰胺作用研究进展:揭示其对衰老、疾病进展、法医学及治疗效果的影响
Proteomes. 2025 Jun 5;13(2):24. doi: 10.3390/proteomes13020024.
2
Eye lens β-crystallins are predicted by native ion mobility-mass spectrometry and computations to form compact higher-ordered heterooligomers.眼晶状体β-晶体蛋白通过天然离子淌度-质谱和计算预测形成紧密的高等阶异源寡聚物。
Structure. 2023 Sep 7;31(9):1052-1064.e3. doi: 10.1016/j.str.2023.06.013. Epub 2023 Jul 14.
3
In Vivo Quasi-Elastic Light Scattering Eye Scanner Detects Molecular Aging in Humans.
体内准弹性光散射眼扫描仪可检测人类的分子衰老。
J Gerontol A Biol Sci Med Sci. 2020 Sep 16;75(9):e53-e62. doi: 10.1093/gerona/glaa121.
4
Age estimation based on aspartic acid racemization in dentine: what about caries-affected teeth?基于牙本质中天冬氨酸消旋化的年龄估计:那么受龋影响的牙齿呢?
Int J Legal Med. 2018 Mar;132(2):623-628. doi: 10.1007/s00414-017-1667-6. Epub 2017 Aug 19.
5
Isoaspartic acid is present at specific sites in myelin basic protein from multiple sclerosis patients: could this represent a trigger for disease onset?多发性硬化症患者髓鞘碱性蛋白的特定部位存在异天冬氨酸:这是否代表疾病发作的一个诱因?
Acta Neuropathol Commun. 2016 Aug 12;4(1):83. doi: 10.1186/s40478-016-0348-x.
6
Old Proteins in Man: A Field in its Infancy.人类体内的衰老蛋白质:一个尚处起步阶段的领域。
Trends Biochem Sci. 2016 Aug;41(8):654-664. doi: 10.1016/j.tibs.2016.06.004. Epub 2016 Jul 11.
7
Understanding the physiology of the ageing individual: computational modelling of changes in metabolism and endurance.了解衰老个体的生理学:新陈代谢和耐力变化的计算模型
Interface Focus. 2016 Apr 6;6(2):20150079. doi: 10.1098/rsfs.2015.0079.
8
The etiology of human age-related cataract. Proteins don't last forever.人类年龄相关性白内障的病因。蛋白质不会永远存在。
Biochim Biophys Acta. 2016 Jan;1860(1 Pt B):192-8. doi: 10.1016/j.bbagen.2015.08.016. Epub 2015 Aug 28.
9
Effects of photobleaching on selected advanced glycation end products in the human lens.光漂白对人晶状体中选定的晚期糖基化终产物的影响。
BMC Res Notes. 2015 Jan 16;8:5. doi: 10.1186/s13104-015-0977-3.
10
Identification of long-lived proteins retained in cells undergoing repeated asymmetric divisions.在经历反复不对称分裂的细胞中保留的长寿蛋白质的鉴定。
Proc Natl Acad Sci U S A. 2014 Sep 30;111(39):14019-26. doi: 10.1073/pnas.1416079111. Epub 2014 Sep 16.